Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[Glycogenosis type IX caused by a novel mutation of phosphorylase kinase α subunit: a family analysis].

Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology - 20 Apr 2017

Zhang M H, Wang H J, Zhang P, Gong J Y, Wang J S

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Glycogen Storage Disease
Share to Liver
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Open in PubMed Open full text

Identifiers

PMID: 28494553
DOI: 10.3760/cma.j.issn.1007-3418.2017.04.015
PMCID: PMC12813985

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Glycogenosis type IX caused by a novel mutation of phosphorylase kinase α subunit: a family analysis].PMID 28494553Read ↗

[Different phenotypes of type IXb glycogenosis (phosphorylase-b-kinase deficiency) in adult- and early childhood].Semantic proximity Read ↗

Molecular aspects of glycogen storage disease type Ia in Turkish patients: a novel mutation in the glucose-6-phosphatase gene.Semantic proximity Read ↗

[Phosphorylase b kinase deficiency].Semantic proximity Read ↗

[Glycogenosis type V (muscle phosphorylase deficiency)].Semantic proximity Read ↗

[Splicing abnormalities caused by a novel mutation in the PHKA2 gene in children with glycogen storage disease type IX].Semantic proximity Read ↗

[Glycogenosis type IV (branching enzyme deficiency, amylopectinosis, Andersen disease, polyglucosan body disease)].Semantic proximity Read ↗

Glycogen storage disorder types IX: the mutation spectrum and ethnic distribution.Semantic proximity Read ↗

[A Chinese patient with glycogen storage disease type Ib caused by mutations in the glucose-6-phosphate translocase gene].Semantic proximity Read ↗

[Genetic analysis of a child with glycogen storage disease type IXa due to a novel variant in PHKA2 gene].Semantic proximity Read ↗

Biochemistry and molecular genetics of human glycogenoses: an overview.Semantic proximity Read ↗

Novel sequence of PHKG2 mutation associated with first case of glycogen storage disease type IXc in Syria: a case reportSemantic proximity Read ↗

Identification of a novel deletion mutation in PHKA2 in a taiwanese patient with type IXa glycogen storage disease.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.